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首页> 外文期刊>ACS medicinal chemistry letters >Identification of 1-4-Benzyloxyphenyl)-but-3-enyl-1H-azoles as New Class of Antitubercular and Antimicrobial Agents
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Identification of 1-4-Benzyloxyphenyl)-but-3-enyl-1H-azoles as New Class of Antitubercular and Antimicrobial Agents

机译:1-4-苄氧基苯基丁-3-烯基-1H-唑类药物作为新型抗结核和抗菌剂的鉴定

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摘要

A series of 1-(4-benzyloxyphenyl)-but-3-enyl-1H-azoles has been identified as potent antitubercular agents against Mycobacterium tuberculosis. Synthesis of compounds involved acid catalyzed ring-opening of cyclopropyl ring of phenyl cyclopropyl methanols followed by nucleophilic attack of the azoles on the carbocation intermediates. Several of the compounds 26, 34, and 36 exhibited significant antitubercular activities with MIC value as low as 1.56, 1.56, and 0.61 g/ mL, respectively, comparable to many standard drugs. These compounds were also screened against other strains of bacteria and fungi, and few of them showed good antifungal activity against A. f umigatus, responsible for lung infection.
机译:一系列 1-[(4-苄氧基苯基)-丁-3-烯基]-1H-唑已被确定为抗结核分枝杆菌的有效抗结核药物。化合物的合成涉及苯基环丙基甲醇环丙基环的酸催化开环,然后是唑类对碳正离子中间体的亲核攻击。化合物 26、34 和 36 中的几种表现出显着的抗结核活性,MIC 值分别低至 1.56、1.56 和 0.61 g/mL,与许多标准药物相当。这些化合物还针对其他细菌和真菌菌株进行了筛选,其中很少有化合物对导致肺部感染的 A. f umigatus 表现出良好的抗真菌活性。

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